Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191816Generated: November 3, 2026

Trifluoroacetic acid → 2-((2-(Dimethylamino)phenyl)amino)-4-phenethylbenzoic acid

https://huagongshe.com/reaction/2191816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 2-((2-(dimethylamino)phenyl)amino)-4-phenethylbenzoateHCID 68961327—
Product2-((2-(Dimethylamino)phenyl)amino)-4-phenethylbenzoic acidHCID 57667958—

Reaction Steps

Trifluoroacetic acid 5.0 mL was added to the obtained tert-butyl 2-((2-(dimethylamino)phenyl)amino)-4-phenethylbenzoate, and it was stirred at room temperature for 3 hours. The solvent was removed under reduced pressure, the obtained residue was refined by reversed-phase silica gel column chromatography [eluent; 50-85% acetonitrile/0.1% trifluoroacetic acid aqueous solution], and ethyl acetate, water and saturated sodium hydrogen carbonate aqueous solution were added to it, and it was adjusted to pH6.5. The organic layer was separated and collected,dried over anhydrous magnesium sulfate after washing with saturated sodium chloride aqueous solution, and the solvent was removed under reduced pressure. Hexane was added to the obtained residue, and solid matter was filtrated to give 2-((2-(dimethylamino)phenyl)amino)-4-phenethylbenzoic acid 7.0 mg of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08327467B2
Source datasetuspto-grants-2012_12
ORD IDord-79807aa4e8b248cebfbcc24c3c976d8b
Source noteuspto-grants-2012_12